Canadian data is current through March 2018. All of the data comes from Health Canada, except for the categories Manufacturer Parent Company and Product Classification.
The Parent Company and the Product Classification were added by ICIJ.
The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and Canada.
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Siemens healthcare diagnostics has confirmed an error in the v3.9 software which may affect na+ results on your aqc cartridge (smn 10310323). level 2 & 3 na+ aqc values may be elevated but within the published target ranges. the published aqc target ranges for all other analytes are unaffected. manual quality controls are also unaffected. this software issue has been addressed with a manufacturing change to the aqc cartridges beginning with aqc cartridge lot number aqc/1774 (serial number 1403793825). aqc cartridges used on the rapidpoint 500 and rapidlab 1200 systems are not affected.